Abstract
The authors recruited 19 nonambulant patients with Guillain- Barree syndrome into a pilot, double- blind, randomized, placebo- controlled safety trial of interferon beta 1a ( IFN beta- 1a) ( Rebif). Participants received IFN beta- 1a or placebo subcutaneously three times weekly, 22 mu g for the first week and then 44 mu g for up to 24 weeks, in addition to IV immunoglobulin ( IVIg). IFN beta did not have any unexpected interaction with IVIg and there was no significant difference in rate of improvement.
Original language | English |
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Pages (from-to) | 1282 - 1284 |
Number of pages | 3 |
Journal | Neurology |
Volume | 61 |
Issue number | 9 |
Publication status | Published - 2003 |